US20100203234A1 - Shape memory alloy actuators - Google Patents
Shape memory alloy actuators Download PDFInfo
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- US20100203234A1 US20100203234A1 US12/702,982 US70298210A US2010203234A1 US 20100203234 A1 US20100203234 A1 US 20100203234A1 US 70298210 A US70298210 A US 70298210A US 2010203234 A1 US2010203234 A1 US 2010203234A1
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
- F16K31/00—Actuating devices; Operating means; Releasing devices
- F16K31/02—Actuating devices; Operating means; Releasing devices electric; magnetic
- F16K31/025—Actuating devices; Operating means; Releasing devices electric; magnetic actuated by thermo-electric means
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/02—Inorganic materials
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/08—Materials for coatings
- A61L29/085—Macromolecular materials
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F03—MACHINES OR ENGINES FOR LIQUIDS; WIND, SPRING, OR WEIGHT MOTORS; PRODUCING MECHANICAL POWER OR A REACTIVE PROPULSIVE THRUST, NOT OTHERWISE PROVIDED FOR
- F03G—SPRING, WEIGHT, INERTIA OR LIKE MOTORS; MECHANICAL-POWER PRODUCING DEVICES OR MECHANISMS, NOT OTHERWISE PROVIDED FOR OR USING ENERGY SOURCES NOT OTHERWISE PROVIDED FOR
- F03G7/00—Mechanical-power-producing mechanisms, not otherwise provided for or using energy sources not otherwise provided for
- F03G7/06—Mechanical-power-producing mechanisms, not otherwise provided for or using energy sources not otherwise provided for using expansion or contraction of bodies due to heating, cooling, moistening, drying or the like
- F03G7/065—Mechanical-power-producing mechanisms, not otherwise provided for or using energy sources not otherwise provided for using expansion or contraction of bodies due to heating, cooling, moistening, drying or the like using a shape memory element
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/16—Materials with shape-memory or superelastic properties
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0043—Catheters; Hollow probes characterised by structural features
- A61M2025/0063—Catheters; Hollow probes characterised by structural features having means, e.g. stylets, mandrils, rods or wires to reinforce or adjust temporarily the stiffness, column strength or pushability of catheters which are already inserted into the human body
- A61M2025/0064—Catheters; Hollow probes characterised by structural features having means, e.g. stylets, mandrils, rods or wires to reinforce or adjust temporarily the stiffness, column strength or pushability of catheters which are already inserted into the human body which become stiffer or softer when heated
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
- A61M2025/09133—Guide wires having specific material compositions or coatings; Materials with specific mechanical behaviours, e.g. stiffness, strength to transmit torque
- A61M2025/09141—Guide wires having specific material compositions or coatings; Materials with specific mechanical behaviours, e.g. stiffness, strength to transmit torque made of shape memory alloys which take a particular shape at a certain temperature
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/02—General characteristics of the apparatus characterised by a particular materials
- A61M2205/0266—Shape memory materials
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T83/00—Cutting
- Y10T83/02—Other than completely through work thickness
- Y10T83/0304—Grooving
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- Heart & Thoracic Surgery (AREA)
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Abstract
A shape memory alloy (SMA) actuator includes a groove formed in a surface of a shape memory alloy (SMA) substrate establishing a trace pattern for a layer of conductive material formed over an electrically insulative layer. The trace pattern includes a first end, a second end, and a heating element disposed between the first and second ends. The SMA substrate is trained to deform at a transition temperature achieved when electricity is conducted through the conductive material via first and second interconnect pads terminating the first and second ends of the trace pattern.
Description
- This application is a continuation of U.S. patent application Ser. No. 10/410,546, filed Apr. 9, 2003 entitled “SHAPE MEMORY ALLOY ACTUATORS”, herein incorporated by reference in its entirety.
- Cross-reference is hereby made to commonly assigned related U.S. Pat. No. 6,832,478 to David Anderson, et al., entitled “Shape Memory Alloy Actuators” (Attorney Docket No. P0009579.00).
- Embodiments of the present invention relate generally to shape memory alloy (SMA) actuators and more particularly to means for forming SMA actuators and incorporating such actuators into elongated medical devices.
- The term SMA is applied to a group of metallic materials which, when subjected to appropriate thermal loading, are able to return to a previously defined shape or size. Generally an SMA material may be plastically deformed at some relatively low temperature and will return to a pre-deformation shape upon exposure to some higher temperature by means of a micro-structural transformation from a flexible martensitic phase at the low temperature to an austenitic phase at a higher temperature. The temperature at which the transformation takes place is known as the activation temperature. In one example, a TiNi alloy has an activation temperature of approximately 70° C. An SMA is “trained” into a particular shape by heating it well beyond its activation temperature to its annealing temperature where it is held for a period of time. In one example, a TiNi alloy is constrained in a desired shape and then heated to 510° C. and held at that temperature for approximately fifteen minutes.
- In the field of medical devices SMA materials, for example TiNi alloys, such as Nitinol, or Cu alloys, may form a basis for actuators designed to impart controlled deformation to elongated interventional devices. Examples of these devices include delivery catheters, guide wires, electrophysiology catheters, ablation catheters, and electrical leads, all of which require a degree of steering to access target sites within a body; that steering is facilitated by an SMA actuator. An SMA actuator within an interventional device typically includes a strip of SMA material extending along a portion of a length of the device and one or more resistive heating elements through which electrical current is directed. Each heating element is attached to a surface of the SMA strip, in proximity to portions of the SMA strip that have been trained to bend upon application of thermal loading. A layer of electrically insulating material is disposed over a portion of the SMA strip on which a conductive material is deposited or applied in a trace pattern forming the heating element. Electrical current is directed through the conductive trace from wires attached to interconnect pads that terminate each end of the trace. In this way, the SMA material is heat activated while insulated from the electrical current. It is important that, during many cycles of activation, the insulative layer does not crack or delaminate from the surface of the SMA strip.
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FIG. 1A is a plan view including a partial section of an elongated medical device including an SMA actuator. -
FIG. 1B is a plan view of the exemplary device ofFIG. 1A wherein a current has been passed through heating elements of the SMA actuator. -
FIG. 1C is a plan view including a partial section of another embodiment of an elongated medical device including an SMA actuator. -
FIG. 1D is a plan view of the exemplary device ofFIG. 1C wherein a current has been passed through heating elements of the SMA actuator. -
FIG. 2A is a perspective view of an SMA substrate or strip that would be incorporated in an SMA actuator. -
FIG. 2B is a plan view of a portion of a surface of an SMA actuator. -
FIG. 3 is a section view through a portion of an SMA actuator according an embodiment of the present invention. -
FIG. 4 is a section view through a portion of an SMA actuator according to an alternate embodiment of the present invention. -
FIGS. 5A-D are section views illustrating steps, according to embodiments of the present invention, for forming the SMA actuator illustrated inFIG. 4 . -
FIGS. 1A-D illustrate two examples of elongated medical devices each incorporating an SMA actuator, wherein each actuator serves to control deformation of a portion of each device.FIG. 1A is a plan view with partial section of an elongatedmedical device 300 including an SMA actuator 56. As illustrated inFIG. 1A ,medical device 300 further includes a shaft 305, ahub 303 terminating a proximal end of shaft 305, andconductor wires 57 coupled to SMA actuator 56. SMA actuator 56, positioned within adistal portion 100 of shaft 305, includes a plurality of heating elements (not shown), electrically insulated from an SMA substrate, through which current flows fed bywires 57;wires 57, extending proximally and joined to electrical contacts (not shown) onhub 303, carry current to heat portions of the SMA substrate to an activation temperature. At the activation temperature, portions of the SMA substrate revert to a trained shape, for example ashape 200 as illustrated inFIG. 1B .FIG. 1B is a plan view of theexemplary device 300 ofFIG. 1A wherein a current has been passed through heating elements of SMA actuator 56, locations of which heating elements correspond tobends shaft 605 in proximity of SMA actuator 56 returnsdistal portion 100 back to a substantially straight form as illustrated inFIG. 1A .Device 300, positioned within a lumen of another elongated medical device, may be used to steer or guide a distal portion of the other device via controlled deformation of actuator 56 at locations corresponding tobends FIG. 1B , or individually, or in paired combinations. -
FIG. 1C is a plan view including a partial section of another embodiment of an elongatedmedical device 600 including anSMA actuator 10 embedded in a portion of a wall 625 of ashaft 605. As illustrated inFIG. 1C ,medical device 600 further includes ahub 603 terminating a proximal end ofshaft 605, alumen 615 extending alongshaft 605, from adistal portion 610 throughhub 603, andconductor wires 17 coupled toSMA actuator 10.SMA actuator 10, positioned withindistal portion 610 ofshaft 605, includes a plurality of heating elements (not shown), electrically insulated from an SMA substrate, through which current flows fed bywires 17;wires 17, extending proximally and joined to electrical contacts (not shown) onhub 603, carry current to heat portions of the SMA substrate to an activation temperature. At the activation temperature, portions of the SMA substrate revert to a trained shape, for example abend 620 as illustrated inFIG. 1D .FIG. 1D is a plan view of theexemplary device 600 ofFIG. 1C wherein a current has been passed through a heating element ofSMA actuator 10, a location of which heating element corresponds to bend 620. When the current is cut, either an external force or a spring element (not shown), for example embedded in a portion of shaft wall 625, returnsdistal portion 610 back to a substantially straight form as illustrated inFIG. 1C .Lumen 615 ofdevice 600, may form a pathway to slideably engage another elongated medical device, guiding the other device via controlled deformation ofdistal portion 610 byactuator 10 resulting inbend 620. -
FIGS. 2A-B illustrate portions of exemplary SMA actuators that may be incorporated into an elongated medical device, forexample device 300 illustrated inFIGS. 1A-B .FIG. 2A is a perspective view of an SMA substrate orstrip 20 that would be incorporated into an SMA actuator, such as SMA actuator 56 illustrated inFIG. 1A . Embodiments of the present invention include an SMA substrate, such asstrip 20, having a thickness between approximately 0.001 inch and approximately 0.1 inch; a width and a length ofstrip 20 depends upon construction and functional requirements of a medical device into whichstrip 20 is integrated. As illustrated inFIG. 2A strip 20 includes asurface 500, which according to embodiments of the present invention includes a layer of an inorganic electrically insulative material formed or deposited directly thereon, examples of which include oxides such as silicon oxide, titanium oxide, or aluminum oxide, nitrides such as boron nitride, silicon nitride, titanium nitride, or aluminum nitride, and carbides such as silicon carbide, titanium carbide, or aluminum carbide. Means for forming the inorganic material layer are well know to those skilled the art and include vacuum deposition methods, such as sputtering, evaporative metalization, plasma assisted vapor deposition, or chemical vapor deposition; other methods include precipitation coating and printing followed by sintering. In an alternate embodiment an SMA substrate, such asstrip 20, is a TiNi alloy and a native oxide of the TiNi alloy forms the layer of inorganic electrically insulative material; the native oxide may be chemically, electrochemically or thermally formed onsurface 500. In yet another embodiment, a deposited non-native oxide, nitride, or carbide, such as one selected from those mentioned above, in combination with a native oxide forms the layer of electrically insulative material onsurface 500. - According to embodiments of the present invention, an SMA substrate, such as
strip 20, is trained to bend, for example in the direction indicated by arrow A inFIG. 2A , after deposition or formation of an inorganic electrically insulative layer uponsurface 500, since the inorganic insulative layer will not break down under training temperatures. Training temperatures for TiNi alloys range between approximately 300° C. and approximately 800° C. Alternately an SMA substrate, such asstrip 20, may be trained to bend before deposition or formation of the inorganic insulative layer if a temperature of the substrate, during a deposition or formation process, is maintained below an activation temperature of the substrate. Furthermore, according to an alternate embodiment, an additional layer of an organic material is deposited over the inorganic layer to form a composite electrically insulative layer. Examples of suitable organic materials include polyimide, parylene, benzocyclobutene (BCB), and fluoropolymers such as polytetrafluoroethylene (PTFE). Means for forming the additional layer are well known to those skilled in the art and include dip coating, spay coating, spin coating, chemical vapor deposition, plasma assisted vapor deposition and screen printing; the additional layer being formed following training of the SMA substrate and at a temperature below an activation temperature of the substrate. An activation temperature for an SMA actuator included in an interventional medical device must be sufficiently high to avoid accidental activation at body temperature; a temperature threshold consistent with this requirement and having a safety factor built in is approximately 60° C. This lower threshold of approximately 60° C. may also prevent accidental activation during shipping of the medical device. An activation temperature must also be sufficiently low to avoid thermal damage to body tissues and fluids; a maximum temperature consistent with this requirement is approximately 100° C., but will depend upon thermal insulation and, or cooling means employed in a medical device incorporating an SMA actuator. -
FIG. 2B is a plan view of a portion of a surface of an SMA actuator 50.FIG. 2B illustrates a group of conductive trace patterns; portions of the conductive trace patterns are formed either on a first layer, a second layer, or between the first and second layer of a multi-layer electrical insulation 1 formed on a surface of an SMA substrate, such asstrip 20 illustrated inFIG. 2A . As illustrated inFIG. 2B , conductive trace pattern includes heating element traces 2, which are formed on first layer of insulation 1, signal traces 4, 5, which are formed on second layer of insulation 1, andconductive vias 3, 9, which traverse second layer in order to electrically couple heating element signal traces 2 on first layer with signal traces 4, 5 on second layer. Each signal trace 4 extends from aninterconnect pad 6 through via 3 to heating element trace 2, while signal trace 5 extends from all heating element traces 2 through vias 9 to a common interconnect pad 7. According to embodiments of the present invention, multi-layer insulation 1 is formed of an inorganic electrically insulative material, examples of which are presented above, deposited or formed directly on the SMA substrate. Portions of conductive trace pattern deposited upon each layer of multi-layer insulation 1, according to one embodiment, are formed of a first layer of titanium, a second layer of gold and a third layer of titanium and eachinterconnect pad 6, 7 is formed of gold deposited upon the second layer of insulation 1. Details regarding pattern designs, application processes, thicknesses, and materials of conductive traces that may be included in embodiments of the present invention are known to those skilled in the arts of VLSI and photolithography. - Section views in
FIGS. 3 and 4 illustrate embodiments of the present invention in two basic forms.FIG. 3 is a section view through a portion of anSMA actuator 30 including one segment of aconductive trace 32 that may be a portion of a heating element trace, such as a heating element trace 2 illustrated inFIG. 2B . As illustrated inFIG. 3 ,SMA actuator 30 further includes an SMA substrate 350, afirst insulative layer 31, electrically isolatingconductive trace 32 from SMA substrate 350, and asecond insulative layer 33 covering and surroundingconductive trace 32 to electrically isolateconductive trace 32 from additional conductive traces that may be included in a pattern, such as the pattern illustrated inFIG. 2B . According to embodiments of the present invention,first insulative layer 31, including an inorganic material, is deposited or formed directly on substrate 350, as described in conjunction withFIG. 2A . Conductive materials are deposited or applied oninsulative layer 31, creatingconductive trace 32, for example by etching, and then secondinsulative layer 33, including an inorganic material, is deposited or applied overconductive trace 32. In an alternate embodiment,second insulative layer 33 includes an organic electrically insulative material; examples of suitable organic materials include polyimide, parylene, benzocyclobutene (BCB), and fluoropolymers such as polytetrafluoroethylene (PTFE). Means for forminginsulative layer 33 include dip coating, spray coating, spin coating, chemical vapor deposition, plasma assisted vapor deposition and screen-printing. Training of SMA substrate 350 may follow or precede formation offirst insulative layer 31, as previously described in conjunction withFIG. 2A . -
FIG. 4 is a section view through a portion of an SMA actuator 40 including one segment of aconductive trace 42. According to alternate embodiments of the present invention, a groove in a surface of an SMA substrate 450 (referenceFIG. 5A ) establishes a pattern forconductive trace 42, the pattern including a heating element trace disposed between signal traces, similar to one of heating element traces 2 and corresponding signal traces 4,5 illustrated inFIG. 2B . As illustrated inFIG. 4 , aninsulative layer 41 is disposed betweenconductive trace 42 andSMA substrate 450 electrically isolatingconductive trace 42 from anSMA substrate 450. According to embodiments of the present invention,insulative layer 41 includes an inorganic material, examples of which are given in conjunction withFIG. 2A , formed directly onSMA substrate 450. Training ofSMA substrate 450 may follow or precede formation offirst insulative layer 41 including an inorganic material, as previously described in conjunction withFIG. 2A . According to alternate embodiments of the present invention,insulative layer 41 includes an organic material, formed directly onSMA substrate 450 following training ofsubstrate 450. Selected organic materials forinsulative layer 41 include those which may be deposited or applied at a temperature below an activation temperature ofSMA substrate 450 and those which will not degrade at the activation temperature ofSMA substrate 450; examples of such materials include polyimide, parylene, benzocyclobutene (BCB), and fluoropolymers such as polytetrafluoroethylene (PTFE). Means for forminginsulative layer 41 include dip coating, spray coating, spin coating, chemical vapor deposition, plasma assisted vapor deposition and screen-printing. -
FIGS. 5A-D are section views illustrating steps, according to embodiments of the present invention, for forming SMA actuator 40 illustrated inFIG. 4 .FIG. 5A illustratesSMA substrate 450 including a groove 510 formed in asurface 515; groove 510 is formed, for example by a machining process.FIG. 5B illustrates a layer of electrically insulative material 511 formed onsurface 515 and within groove 510.FIG. 5C illustrates a layer ofconductive material 512 formed over layer of insulative material 511.FIG. 5D illustratesinsulative layer 41 andconductive trace 42 left in groove 510 after polishing excess insulative material 511 andconductive material 512 fromsurface 515. As illustrated inFIG. 5D ,conductive trace 42 is flush withsurface 515 following polishing; in one example, according to this embodiment, groove 510 is formed having a width of approximately 25 micrometer and a depth of approximately 1.2 micrometer approximately matching a predetermined combined thickness ofinsulative layer 41 andconductive trace 42. According to alternate embodiments of the present invention, groove 510 is formed deeper than a resultant combined thickness of theinsulative layer 41 andconductive trace 42 so that conductive trace is recessed fromsurface 515. - Minimum theoretical thicknesses having sufficient dielectric strength for operating voltages of 100V, 10V, and 1V applied across conductive traces on SMA actuators were calculated for insulating layers of Silicon Nitride, Aluminum Nitride, Boron Nitride, and polyimide according to the following formula:
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Thickness=voltage/dielectric strength. - A dielectric strength for Silicon Nitride was estimated to be 17700 volts/millimeter; a dielectric strength for Aluminum Nitride was estimated to be 15,000 volts/millimeter; a dielectric strength for Boron Nitride was estimated to be 3,750 volts/millimeter; a dielectric strength for polyimide was estimated to be 157,500 volts/millimeter. Results are presented in Table 1.
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TABLE 1 Thickness, Thickness, Thickness, 100 V 10 V 1 V (micrometer) (micrometer) (micrometer) Silicon Nitride 5.65 0.56 0.06 Aluminum Nitride 6.67 0.67 0.07 Boron Nitride 26.7 2.67 0.27 Polyimide 0.64 0.064 0.0064 - Finally, it will be appreciated by those skilled in the art that numerous alternative forms of SMA substrates and trace patterns included in SMA actuators and employed in medical devices are within the spirit of the present invention. For example, SMA actuators according to the present invention can include conductive trace patterns on two or more surfaces of an SMA substrate or an additional layer or layers of non-SMA material joined to an SMA substrate, which serve to enhance biocompatibility or radiopacity in a medical device application. Hence, descriptions of particular embodiments provided herein are intended as exemplary, not limiting, with regard to the following claims.
Claims (4)
1. A method for manufacturing a shape memory alloy (SMA) actuator, comprising forming a groove on a surface of an SMA substrate to establish a trace pattern.
2. The method of claim 1 , further comprising forming a layer of electrically insulative material on the surface of the SMA substrate including the groove.
3. The method of claim 2 , further comprising forming a layer of conductive material over the insulative layer.
4. The method of claim 3 , further comprising removing insulative material and conductive material from a portion of the surface of the SMA substrate not including the groove, leaving behind insulative material and conductive material in the groove.
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US10/410,546 US7658709B2 (en) | 2003-04-09 | 2003-04-09 | Shape memory alloy actuators |
US12/702,982 US20100203234A1 (en) | 2003-04-09 | 2010-02-09 | Shape memory alloy actuators |
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US9318593B2 (en) | 2014-07-21 | 2016-04-19 | Transphorm Inc. | Forming enhancement mode III-nitride devices |
US9443938B2 (en) | 2013-07-19 | 2016-09-13 | Transphorm Inc. | III-nitride transistor including a p-type depleting layer |
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Also Published As
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WO2004091681A1 (en) | 2004-10-28 |
US20040204676A1 (en) | 2004-10-14 |
US7658709B2 (en) | 2010-02-09 |
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